Variant report
| Variant | rs1066397 |
|---|---|
| Chromosome Location | chr12:67719914-67719915 |
| allele | A/C |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:67706600-67720600 | Weak transcription | Primary mononuclear cells fromperipheralblood | Blood |
| 2 | chr12:67711200-67721400 | Weak transcription | Fetal Brain Female | brain |
| 3 | chr12:67713400-67725000 | Weak transcription | Dnd41 | blood |
| 4 | chr12:67713600-67720800 | Weak transcription | Skeletal Muscle Male | skeletal muscle |
| 5 | chr12:67716600-67732000 | Weak transcription | HMEC | breast |
| 6 | chr12:67716600-67748000 | Weak transcription | HSMM | muscle |
| 7 | chr12:67717000-67721400 | Weak transcription | Thymus | Thymus |
| 8 | chr12:67717400-67731400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 9 | chr12:67717600-67720800 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
| 10 | chr12:67718000-67720800 | Weak transcription | Skeletal Muscle Female | skeletal muscle |
| 11 | chr12:67718200-67721000 | Weak transcription | Psoas Muscle | Psoas |
